2,2,6,6-tetramethylpiperidin-4-ol

CC1(C)CC(OC(=O)CS(=O)(=O)C(C)(C)C)CC(C)(C)N1
Reaction #54461
2,2,6,6-tetramethyl-4-piperidinyl t-butyl-sulphonyl-acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC1(C)CC(OC(=O)CCc2cc(-n3nc4ccc(S(=O)(=O)c5ccccc5)cc4n3)c(O)c(C(C)(C)C)c2)CC(C)(C)N1
Reaction #56605
orange oil
Ausbeute 103.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1(C)CC(OCC2CO2)CC(C)(C)N1
Reaction #80669
2,2,6,6-tetramethyl-4-(2,3-epoxypropoxy)piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC1(C)CC(O)CC(C)(C)N1Cc1ccccc1
Reaction #179984
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)CC(OC(=O)CCc2cc(-n3nc4ccc(S(=O)(=O)c5ccccc5)cc4n3)c(O)c(C(C)(C)C)c2)CC(C)(C)N1
Reaction #183783
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220832
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220833
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220834
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1(C)CC(O)CC(C)(C)N1CC(O)c1ccccc1
Reaction #221668
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)CC(O)CC(C)(C)N1C#N
Reaction #227066
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(NC1CC(C)(C)NC(C)(C)C1)C(=O)OC1CC(C)(C)NC(C)(C)C1
Reaction #236528
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)CC(OC(=O)CS(=O)(=O)C(C)(C)C)CC(C)(C)N1
Reaction #248422
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCN1C(C)(C)CC(O)CC1(C)C
Reaction #256156
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCC(=O)NCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1
Reaction #262053
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1(C)CC(O)CC(C)(C)N1O
Reaction #402165
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1(C)CC(OC(=O)CCC(C)(c2ccc(O)c(C(C)(C)C)c2)c2ccc(O)c(C(C)(C)C)c2)CC(C)(C)N1
Reaction #445412
2,2,6,6-tetramethylpiperidin-4-yl 4,4-bis-(3-tert.-butyl-4-hydroxyphenyl)-valerate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_08
CC1(C)CC(O)CC(C)(C)N1O
Reaction #446759
needles
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
CC1(C)CC(OCC2CO2)CC(C)(C)N1
Reaction #528292
2,2,6,6-tetramethyl-4-(2,3-epoxypropoxy)piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1.Cl
Reaction #578710
TMPH hydrochloride
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CCCCCCCCCCCCN1C(C)(C)CC(O)CC1(C)C
Reaction #684729
1-n-dodecyl-2,2,6,6-tetramethylpiperidin-4-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_03
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